REGULATION OF ANTIBODY HETEROGENEITY BY SUPPRESSOR T CELLS - DIMINISHING SUPPRESSOR T CELL ACTIVITY INCREASES NUMBER OF DINITROPHENYL CLONES IN MICE IMMUNIZED WITH DINITROPHENYLPOLY(GLU,LYS,PHE) OR DINITROPHENYL-POLY(GLU,LYS,ALA)

被引:15
作者
KIPPS, TJ
BENACERRAF, B
DORF, ME
机构
关键词
D O I
10.1073/pnas.75.6.2914
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The anti-hapten responses to the dinitrophenyl (Dnp) conjugate of the random linear terpolymers poly(L-Glu,LLys,LPhe), Glphi, or poly(LGlu,LLys,LAla), GLA, are of highly restricted heterogeneity. Thus, individual mice of most responder strains express an average of two to four anti-Dnp clones to Dnp-GLphi or Dnp-GLA, as measured by isoelectric focusing techniques. To explore whether suppressor T cells regulate the heterogeneity of the anti-hapten response to Dnp conjugates of these polypeptides, various procedures aimed at reducing suppressor T-cell activity were tesed for their ability to alter the restricted isoelectric focusing spectrotypes. These procedures, such as adult thymectomy, administration of low doses of cyclophosphamide, and in vivo treatment with anti-I-J antisera, significantly increased the magnitude and heterogeneity of the anti-Dnp antibody response to Dnp-GLphi and Dnp-GLA in strains of mice that possessed responder Ir genes. Such methods failed to alter the nonresponder status of mice that lacked the appropriate Ir genes. Thus, in systems under Ir gene control suppressor T-cell mechanisms appear to be involved in the regulation of the heterogeneity of hapten-specific B-cell responses.
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页码:2914 / 2917
页数:4
相关论文
共 19 条
[1]   ISOELECTRIC FOCUSING IN POLYACRYLAMIDE GEL AND ITS APPLICATION TO IMMUNOGLOBULINS [J].
AWDEH, ZL ;
WILLIAMSON, AR ;
ASKONAS, BA .
NATURE, 1968, 219 (5149) :66-+
[2]  
CANTOR H, 1976, COLD SPRING HARB SYM, V41, P23
[3]   IMMUNOREGULATORY CIRCUITS AMONG T-CELL SETS .2. PHYSIOLOGIC ROLE OF FEEDBACK INHIBITION INVIVO - ABSENCE IN NZB MICE [J].
CANTOR, H ;
MCVAYBOUDREAU, L ;
HUGENBERGER, J ;
NAIDORF, K ;
SHEN, FW ;
GERSHON, RK .
JOURNAL OF EXPERIMENTAL MEDICINE, 1978, 147 (04) :1116-1125
[4]   GENETIC-CONTROL OF SPECIFIC IMMUNE SUPPRESSION .4. RESPONSIVENESS TO RANDOM COPOLYMER L-GLUTAMIC ACID 50 L-TYROSINE 50 INDUCED IN BALB-C MICE BY CYCLOPHOSPHAMIDE [J].
DEBRE, P ;
WALTENBAUGH, C ;
DORF, ME ;
BENACERRAF, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 1976, 144 (01) :277-281
[5]  
Dorf M. E., 1977, Immune system: genetics and regulation., P469
[6]   COMPLEMENTATION OF H-2-LINKED IR GENES IN MOUSE [J].
DORF, ME ;
BENACERRAF, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (09) :3671-3675
[7]  
DORF ME, 1975, J EXP MED, V141, P1459
[8]   MAPPING OF IMMUNE-RESPONSE GENES IN MAJOR HISTOCOMPATIBILITY COMPLEX OF RHESUS-MONKEY [J].
DORF, ME ;
BALNER, H ;
BENACERRAF, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 1975, 142 (03) :673-693
[9]  
DUNHAM EK, 1973, J IMMUNOL, V111, P1621
[10]   SUPPRESSIVE EFFECT OF CARRIER PRIMING ON RESPONSE TO A HAPTEN-CARRIER CONJUGATE [J].
ELSON, CJ ;
TAYLOR, RB .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1974, 4 (10) :682-687